The InterMed Group, an Alachua, Fla.-based provider of scalable healthcare technology management services, announced the recent certification to ISO 13485:2016, a testimony that InterMed’s quality management system meets the most current standards for the service and sale of medical devices as set forth by the International Organization for Standardization (ISO).
ISO 13485 is a rigorous standard now considered to be the inline requirement for medical device manufacturers and service providers. For an organization of the InterMed Group’s size, to comply necessitates an ongoing team effort and tremendous commitment at all levels of the organization.
“Risk management is heavily emphasized in ISO 13485, demanding detailed and effective communications with our colleagues and customers. This aligns with InterMed’s core values and enhances customer and patient relationships,” says Dave Morgan, quality manager for the InterMed group. “Customers can be confident that InterMed takes a risk-based approach with patient safety as a priority, including assurance that we contribute great value toward their legal and regulatory compliance efforts.”
For more information, visit the Intermed Group.
